Fabscout Entertainment, Inc
Complete recall history across all FDA and CPSC categories — 5 total recalls
Fabscout Entertainment, Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Drug Recalls (5)
FDA drug safety enforcement actions by Fabscout Entertainment, Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Aug 14, 2013 | Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet She... | Marketed without an Approved NDA/ANDA: product found to contain undeclared si... | Class I |
| Aug 14, 2013 | PRO POWER MAX Natural Energy Enhancer, ALL NATURAL HERBS, supplied in 1 capsu... | Marketed without an Approved NDA/ANDA: product found to contain undeclared si... | Class I |
| Aug 14, 2013 | 72HP MAXIMUM POTENCY MALE SEXUAL ENHANCEMENT, Dietary Supplement, supplied in... | Marketed without an Approved NDA/ANDA: products were found to contain undecla... | Class I |
| Jun 27, 2013 | Clalis capsules, 50 mg, 6 -count bottle ( labeling is in foreign language) | Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the F... | Class I |
| Jun 27, 2013 | Silver Sword capsules, 180 mg, 16-count clamshell tin, UPC 1 234658 970128 1... | Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the F... | Class I |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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